Faldaprevir (BI 201335), deleobuvir (BI 207127) and ribavirin oral therapy for treatment-naive HCV genotype 1: SOUND-C1 final results

Faldaprevir (BI 201335) and deleobuvir (BI 207127) are direct-acting antiviral agents under development for the treatment of chronic HCV infection. This article describes the final results of the Phase Ib SOUND-C1 study that evaluated the interferon-free oral combination of faldaprevir, deleobuvir a...

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Veröffentlicht in:Antiviral therapy 2013-01, Vol.18 (8), p.1015-1019
Hauptverfasser: ZEUZEM, Stefan, ASSELAH, Tarik, BRONOWICKI, Jean-Pierre, ROBERTS, Stuart, ARASTEH, Keikawus, ZOULIM, Fabien, HEIM, Markus, STERN, Jerry O, NEHMIZ, Gerhard, KUKOLJ, George, BÖCHER, Wulf O, MENSA, Federico J, ANGUS, Peter, ZARSKI, Jean-Pierre, LARREY, Dominique, MÜLLHAUPT, Beat, GANE, Ed, SCHUCHMANN, Marcus, LOHSE, Ansgar W, POL, Stanislas
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Sprache:eng
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Zusammenfassung:Faldaprevir (BI 201335) and deleobuvir (BI 207127) are direct-acting antiviral agents under development for the treatment of chronic HCV infection. This article describes the final results of the Phase Ib SOUND-C1 study that evaluated the interferon-free oral combination of faldaprevir, deleobuvir and ribavirin in 32 treatment-naive patients infected with HCV genotype 1. Patients were randomized to receive deleobuvir 400 mg (n=15) or 600 mg (n=17) three times daily plus faldaprevir 120 mg once daily and weight-based ribavirin for 4 weeks. Interferon-free therapy was followed by response-guided faldaprevir plus pegylated interferon-α2a/ribavirin to week 24 or 48. At week 4, 73% (11/15) and 100% (17/17) of patients in the deleobuvir 400 mg and 600 mg groups achieved HCV RNA
ISSN:1359-6535
2040-2058
DOI:10.3851/IMP2567